Vitrea View
K-Number: K163232 · 2017-07-21
ApplicantVital Images, Inc.
Decision Date2017-07-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Vitrea View is a medical device manufactured by Vital Images, Inc.. It received FDA 510(k) clearance on 2017-07-21 under approval number K163232. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vitrea View?
Vitrea View is a medical device that received FDA 510(k) clearance on 2017-07-21. It is manufactured by Vital Images, Inc.. The 510(k) number is K163232.
When was Vitrea View approved by the FDA?
Vitrea View received FDA 510(k) clearance on 2017-07-21, under approval number K163232.
What company makes Vitrea View?
Vitrea View is manufactured by Vital Images, Inc..
What is the FDA product code for Vitrea View?
The FDA product code for Vitrea View is LLZ.
Other Devices by Vital Images, Inc.
Related Devices (Code: LLZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.